Bone markers in polycystic ovary syndrome: A multicentre study

Clin Endocrinol (Oxf). 2017 Dec;87(6):673-679. doi: 10.1111/cen.13456. Epub 2017 Sep 21.

Abstract

Objective: Hyperandrogenism, hyperinsulinaemia and obesity, known characteristics of polycystic ovary syndrome (PCOS), may influence bone mineral density and biochemical markers of bone turnover (BTMs) can provide a noninvasive assessment of bone turnover. To this end, the serum concentrations of BTMs and 25-hydroxyvitamin D (25OHD) were analysed in women with PCOS, and their possible associations with metabolic parameters of PCOS were determined.

Subjects and methods: Bone formation markers procollagen type I amino-terminal propeptide (PINP) and osteocalcin (OC), and bone resorption marker carboxy-terminal cross-linking telopeptide of type I collagen (CTX), along with 25OHD, were measured in 298 women with PCOS and 194 healthy controls.

Results: Serum levels of PINP (47.0 ± 20.2 vs 58.1 ± 28.6 μg/L, P < .001) and OC (18.2 ± 7.5 vs 20.6 ± 9.8 μg/L, P < .001) were decreased in women with PCOS compared with controls, whereas no significant differences were found in CTX and 25OHD levels. Age-stratified analyses suggested that PINP (50.5 ± 21.7 vs 68.2 ± 26.6 μg/L, P < .001) and OC levels (20.4 ± 7.6 vs 25.5 ± 9.6 μg/L, P < .001) were decreased only in the younger age group (≤30 years) women with PCOS compared with controls. The formation markers and resorption marker decreased with age in both study groups.

Conclusions: Bone formation markers were decreased in younger women with PCOS when compared with healthy women, which may affect bone mass in these women.

Keywords: biochemical markers of bone turnover; carboxy-terminal cross-linking telopeptide of type I collagen; osteocalcin; polycystic ovary syndrome; procollagen type I amino-terminal propeptide.

Publication types

  • Multicenter Study

MeSH terms

  • Adult
  • Biomarkers / metabolism
  • Bone Density / physiology
  • Bone Remodeling / physiology
  • Bone and Bones / metabolism*
  • Bone and Bones / pathology
  • Collagen Type I / metabolism
  • Female
  • Humans
  • Middle Aged
  • Osteocalcin / metabolism
  • Polycystic Ovary Syndrome / metabolism*
  • Polycystic Ovary Syndrome / pathology
  • Vitamin D / analogs & derivatives
  • Vitamin D / metabolism
  • Young Adult

Substances

  • Biomarkers
  • Collagen Type I
  • Osteocalcin
  • Vitamin D
  • 25-hydroxyvitamin D